Aug 2026· Langmuir· Vol 42 35, pp.
25697-25709
· 0 citations· 31 references
Medicine
Abstract
Silicon-graphite (Si/C) composite anodes are promising for next-generation lithium-ion batteries because of their high capacity and industrial compatibility; however, their practical application is hindered by unstable interfacial chemistry and electrode degradation associated with the large volume changes of silicon during cycling. Herein, an interface-adaptive polymer binder, poly(2-acrylamido-2-methylpropanesulfonic acid-co-2-ethylhexyl acrylate-co-acrylic acid) [P(AMPS-co-2-EHA-co-AA), PAEA], is developed to stabilize the heterogeneous Si/C interface through synergistic molecular interactions. PAEA integrates amide, lithium sulfonate, and lithium carboxylate moieties within a single polymer network, enabling reversible hydrogen bonding, ionic interactions, Li+ affinity, and adhesion to hydroxylated Si surfaces. These functional groups establish a multisite adsorption network across Si-rich and carbon domains, thereby enhancing interparticle cohesion and maintaining interfacial contact during cycling. Meanwhile, the lithium sulfonate and carboxylate moieties regulate the local Li+ distribution and facilitate interfacial ion transport, which helps reduce polarization and homogenize interfacial reactions. The enhanced interfacial affinity between PAEA and Si, together with the regulated Li+ flux, reduces direct electrolyte attack and parasitic side reactions, leading to the formation of a thin (4.65 nm), inorganic-rich SEI containing ROCO2Li, Li2CO3, Li2O, LiF, and LiPOxFy, with a Li+ diffusion coefficient of 16.3 × 10-6 cm2 s-1. This interfacial layer contributes to the stabilization of the electrode/electrolyte interface and suppresses continuous SEI growth and structural degradation during cycling. The PAEA-based electrode delivers a capacity of 633.3 mAh g-1 with 82.6% retention after 400 cycles at 0.5 C and maintains a capacity of 633.8 mAh g-1 at 1 C. Furthermore, high-loading pouch-type full cells paired with LiNi0.8Co0.1Mn0.1O2 cathodes retain 79.7% of their initial capacity after 200 cycles, demonstrating the potential of PAEA as a binder for Si/C-based lithium-ion batteries.
The development of lithium-oxygen (Li-O2) batteries, which possess high theoretical energy density, has long been hindered by safety issues and parasitic reactions arising from conventional liquid electrolytes. Gel polymer electrolytes (GPEs) have emerged as a promising alternative to settle these issues; however, th...
Bing Gan, Zheng-Zhou Tao, Jia-Cheng Wu et al.· ACS Applied Energy Materials· 0 citations
Unstable native solid electrolyte interphase (SEI), non-uniform Li+ flux, and dendritic Li growth severely restrict the practical use of lithium metal anodes. Herein, we report a porphyrin–perylene imide porous organic polymer (TP-POP) as an electrolyte-decomposition-directing artificial interphase for stable lithium...
Su-Qing Wei, Ling-Cai Zeng, Jie-Ying Hua et al.· Industrial & Engineering...· 0 citations
The development of cost-effective and durable anode materials derived from renewable biomass is essential for practical lithium- and sodium-ion batteries (LIBs/SIBs). However, conventional strategies for integrating high-capacity metal oxides with biomass carbon often suffer from weak oxide–carbon adhesion, nanoparticl...
Li1.3Al0.3Ti1.7(PO4)3 (LATP)-based all-solid-state lithium metal batteries (ASSLMBs) hold exceptional promise for achieving high energy density and excellent safety, yet their practical application is severely hindered by critical interfacial issues, including poor contact, side reactions, and dendrite growth. Herein,...
Jian Liu, Liu Pei, Ying Song et al.· Small· 0 citations
Metal-organic framework (MOF)-based mixed-matrix membranes (MMMs) are promising for CO2 separation but remain limited by poor filler–polymer compatibility and compromised molecular sieving at high filler loadings. Herein, we developed a hydrogen-bond-mediated molecular interfacial engineering strategy by constructing...
Feng-Ting Yao, Zhi-Xu Yun, Zi-Heng Li et al.· Industrial & Engineering...· 0 citations